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nsv5529908

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,562

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 86 SVs from 30 studies. See in: genome view    
Submitted genomic20,847,054-20,850,615Question Mark
Overlapping variant regions from other studies: 86 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):20,858,376-20,861,937Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5529908Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1620,847,05420,850,615
nsv5529908RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1620,858,37620,861,937

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17704750deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17704750Submitted genomicNC_000016.10:g.208
47054_20850615del
GRCh38 (hg38)NC_000016.10Chr1620,847,05420,850,615
nssv17704750RemappedPerfectNC_000016.9:g.2085
8376_20861937del
GRCh37.p13First PassNC_000016.9Chr1620,858,37620,861,937

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17704750<0.00116404
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